Standardized Perioperative Management of Patients Operated With Acute Abdominal Surgery in a High-risk Emergency Setting
NCT ID: NCT03549624
Last Updated: 2022-11-01
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
1435 participants
OBSERVATIONAL
2018-02-26
2023-09-06
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Transgastric Peritoneoscopy and Appendectomy
NCT00952146
Pathophysiology of Perioperative Fluid Management in Emergency Laparotomy
NCT03997721
Perioperative Metabolic and Hormonal Aspects in Major Emergency Surgery
NCT03482830
Upper Gastrointestinal Perforations: a Nationwide Registry-based Study
NCT06154603
Outcomes After Laparotomy for Penetrating Abdominal Trauma
NCT04536818
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Standard care for these patients in a Swedish setting is a rapid anesthesiological assessment of the patient, preoperative resuscitation - if deemed necessary - followed by surgical intervention. Postoperative care and monitoring dependent on local facilities/routines and individual assessment of the patient and the patients postoperative needs by the surgeon and anaesthetist together.
Recent studies from the United Kingdom indicate that at more standardised protocol with emphasis on six different measures have the possibility to improve postoperative outcome with regard to short term (30 days) mortality. The measures at hand are not new nor untried but the combination of measures including the shortened time to surgery are shown to be beneficial for the patients. The measures are: 1. early so called NEWS-monitoring (measuring of standard physiological parameters); 2. Early start of antibiotics; 3. Rapid (within 6 hours) start of operation; 4. Goal-directed fluid therapy; 5. Intensified post-operative monitoring; 6. The presence of both surgical and anesthesiological specialists in the early care of the patients.
This kind of standardised perioperative protocols has not yet been implemented in Swedish health-care.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Intervention group
All adult (\>18y) patients with the need of an acute laparotomy (within 6 hours) at NÄL.
Patients will be treated with an perioperative regime/protocol consisting of:
1. Early so called NEWS-monitoring (measuring of standard physiological parameters);
2. Early start of antibiotics;
3. Rapid (within 6 hours) start of operation;
4. Goal-directed fluid therapy;
5. Intensified post-operative monitoring;
6. The presence of both surgical and anesthesiological specialists in the early care of the patients.
Standardised protocol for the perioperative management in patients in need of an acute laparotomy
A standardised protocol for the perioperative management of patients including early start of antibiotics and swift surgical intervention as well as an emphasis on repeated monitoring of physiological parameters pre- and post-operatively.
Control group
All patients operated with an acute laparotomy at NÄL the years prior to the study will be retrospectively collected using the hospitals operation management database (Orbit©). Medical data will be collected from the patients' medical charts and outcome data (i.e. mortality, length of hospital stay, surgical complications, ICU-management etc.) will be registered
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Standardised protocol for the perioperative management in patients in need of an acute laparotomy
A standardised protocol for the perioperative management of patients including early start of antibiotics and swift surgical intervention as well as an emphasis on repeated monitoring of physiological parameters pre- and post-operatively.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* Abdominal wall hernias (with no suspicion of ileus or bowel ischemia)
* Appendectomy (Laparoskopically or open)
* Cholecystectomi (Laparoskopically or open)
* Acute thoracotomy
* Akute aortic surgery
* Planned second look-surgery (including change of open abdominal drapings/VAC)
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
NU-Hospital Organization, Sweden
OTHER
Sahlgrenska University Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Mattias Prytz
MD, PhD. Head of Deperatment for Colorectal surgery, Department of Surgery, NU-Hospital Organization
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Mattias Prytz, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Sahlgrenska University Hospital an NU Hospital Oranization
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Department of Surgery, NU-Hospital/NÄL
Trollhättan, Västra Götalandsregionen, Sweden
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Tengberg LT, Bay-Nielsen M, Bisgaard T, Cihoric M, Lauritsen ML, Foss NB; AHA study group. Multidisciplinary perioperative protocol in patients undergoing acute high-risk abdominal surgery. Br J Surg. 2017 Mar;104(4):463-471. doi: 10.1002/bjs.10427. Epub 2017 Jan 23.
Huddart S, Peden CJ, Swart M, McCormick B, Dickinson M, Mohammed MA, Quiney N; ELPQuiC Collaborator Group; ELPQuiC Collaborator Group. Use of a pathway quality improvement care bundle to reduce mortality after emergency laparotomy. Br J Surg. 2015 Jan;102(1):57-66. doi: 10.1002/bjs.9658. Epub 2014 Nov 10.
Jansson Timan T, Hagberg G, Sernert N, Karlsson O, Prytz M. Mortality following emergency laparotomy: a Swedish cohort study. BMC Surg. 2021 Aug 11;21(1):322. doi: 10.1186/s12893-021-01319-8.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Acute laparotomy NU
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.